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MicroRNAs contribute to compensatory β cell expansion during pregnancy and obesity
Cécile Jacovetti, … , Domenico Bosco, Romano Regazzi
Cécile Jacovetti, … , Domenico Bosco, Romano Regazzi
Published September 10, 2012
Citation Information: J Clin Invest. 2012;122(10):3541-3551. https://doi.org/10.1172/JCI64151.
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Research Article Metabolism Article has an altmetric score of 12

MicroRNAs contribute to compensatory β cell expansion during pregnancy and obesity

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Abstract

Pregnancy and obesity are frequently associated with diminished insulin sensitivity, which is normally compensated for by an expansion of the functional β cell mass that prevents chronic hyperglycemia and development of diabetes mellitus. The molecular basis underlying compensatory β cell mass expansion is largely unknown. We found in rodents that β cell mass expansion during pregnancy and obesity is associated with changes in the expression of several islet microRNAs, including miR-338-3p. In isolated pancreatic islets, we recapitulated the decreased miR-338-3p level observed in gestation and obesity by activating the G protein–coupled estrogen receptor GPR30 and the glucagon-like peptide 1 (GLP1) receptor. Blockade of miR-338-3p in β cells using specific anti-miR molecules mimicked gene expression changes occurring during β cell mass expansion and resulted in increased proliferation and improved survival both in vitro and in vivo. These findings point to a major role for miR-338-3p in compensatory β cell mass expansion occurring under different insulin resistance states.

Authors

Cécile Jacovetti, Amar Abderrahmani, Géraldine Parnaud, Jean-Christophe Jonas, Marie-Line Peyot, Marion Cornu, Ross Laybutt, Emmanuelle Meugnier, Sophie Rome, Bernard Thorens, Marc Prentki, Domenico Bosco, Romano Regazzi

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Figure 5

17-β estradiol controls miR-338-3p expression through activation of GPR30.

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17-β estradiol controls miR-338-3p expression through activation of GPR3...
(A–C and E–H) miR-338-3p levels were assessed by qRT-PCR and expressed as a percentage of U6. Rat islets were (A) cultured in the presence of 1 mM dibutyryl cAMP for 0 (Ctrl), 2, 6, and 24 hours; (B) treated for 24 hours with or without 100 nM 17-β estradiol in the presence or absence of 10 μM H89; (E) incubated for 16 hours with vehicle or 100 nM G1; (F) transfected with siRNAs directed against GFP or GPR30, and the following day incubated with or without estradiol for 48 hours; or (H) cultured for 24 hours with 100 nM 17-β estradiol in the presence or absence of 100 nM Fulvestrant. (C) Human islets treated as in B. (G) INS832/13 cells transfected as in F. (D) Expression of GPR30 in islets from nonpregnant rats and of rats at 10, 12, 14, and 20 days of pregnancy and 3 days postpartum. Results are expressed as fold change compared with the level in nonpregnant rats. Data are mean ± SD (n = 3 [A and C]; 4 [B, D, E, G, and H]; 5 [F]). *P < 0.05 vs. control, #P < 0.05 vs. estradiol, ANOVA.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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